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ویرایش:
نویسندگان: Yousaf Ali
سری:
ISBN (شابک) : 9783030806989, 9783030806996
ناشر: Springer
سال نشر: 2022
تعداد صفحات: [421]
زبان: English
فرمت فایل : PDF (درصورت درخواست کاربر به PDF، EPUB یا AZW3 تبدیل می شود)
حجم فایل: 7 Mb
در صورت تبدیل فایل کتاب Rheumatology for Primary Care Providers. A Clinical Casebook به فرمت های PDF، EPUB، AZW3، MOBI و یا DJVU می توانید به پشتیبان اطلاع دهید تا فایل مورد نظر را تبدیل نمایند.
توجه داشته باشید کتاب روماتولوژی برای ارائه دهندگان مراقبت های اولیه. کتاب مورد بالینی نسخه زبان اصلی می باشد و کتاب ترجمه شده به فارسی نمی باشد. وبسایت اینترنشنال لایبرری ارائه دهنده کتاب های زبان اصلی می باشد و هیچ گونه کتاب ترجمه شده یا نوشته شده به فارسی را ارائه نمی دهد.
متون فعلی در روماتولوژی بسیار دقیق است و به طور خاص برای پزشکان روماتولوژی، دستیاران و کارآموزان طراحی شده است. تعداد کمی کتاب به روز وجود دارد که به طور خاص برای پزشکان مراقبت های اولیه در سنگر که به مسائل روماتولوژیک نیز می پردازند، تنظیم شده است. این راهنمای واضح و مختصر برای پزشک پرمشغله ای که در عمل با این اختلالات روماتولوژیک رایج و غیر معمول در تماس است، هدف قرار می گیرد. بسیاری از فصلها یک سناریوی بالینی مشترک را ارائه میکنند و به تعریف بیماری، بروز و شیوع، پاتوفیزیولوژی، تظاهرات رایج، درمان و مشکلات میپردازند. طیف وسیعی از موضوعات در پانزده فصل شامل استئوآرتریت، آرتریت روماتوئید، فیبرومیالژیا، بیماری متابولیک استخوان، نقرس و اسکلرودرمی و غیره گنجانده شده است. نوشته شده توسط متخصصان در این زمینه، روماتولوژی برای ارائه دهندگان مراقبت های اولیه راهنمای قطعی روماتولوژی برای پزشکان مراقبت های اولیه و غیر متخصص است.
Current texts in rheumatology are very detailed and designed specifically for rheumatology physicians, residents and trainees. There are few up-to-date books specifically geared towards the primary care practitioners in the trenches who also deal with rheumatologic issues. This clear and concise guide is targeted at the busy clinician who comes into contact with these common and uncommon rheumatologic disorders in their practice. Many chapters presents a common clinical scenario and move to a definition of the disease, incidence and prevalence, pathophysiology, common manifestations, treatment and pitfalls. A range of topics are included in the fifteen chapters including osteoarthritis, rheumatoid arthritis, fibromyalgia, metabolic bone disease, gout and scleroderma, among others. Written by experts in the field, Rheumatology for Primary Care Providers is the definitive guide to rheumatology for the primary care physician and non-specialist.
Preface Contents Contributors 1: An Approach to a Patient with Joint Pain Introduction Epidemiology The Assessment of a Patient with Joint Pain General History Rheumatological Emergencies Patterns of Rheumatological Conditions Referred Visceral Pain Spinal Disease Periarticular Pain Inflammatory Arthritis Osteoarthritis Muscle Syndromes Connective Tissue Disease (CTD) Pain Syndromes Joint Examination General Examination Musculoskeletal Examination Individual Joint Examination Summary References 2: Osteoarthritis Introduction Pathophysiology Risk Factors Clinical Presentation Knees Hips Hands Diagnostic Testing Management Nonpharmacologic Therapy Exercise and Weight Loss Knee Braces Pharmacologic Therapies Complimentary Therapies Future Direction Summary References 3: Rheumatoid Arthritis Pathophysiology Clinical Presentation and Diagnosis Approach to Patients with Suspected RA Assessment of Clinical Disease Activity Therapy Nonpharmacological Interventions Comorbidities, Vaccination, and Pregnancy Summary References 4: SLE for Primary Care Providers Introduction Pathogenesis Classification Clinical Evaluation General CNS Cardiovascular Gastrointestinal Hematologic Musculoskeletal Pulmonary Renal Skin Laboratory Evaluation Clinical Management Summary and Suggestions References 5: Fibromyalgia for the Primary Care Physician Patient Case Overview What Is Fibromyalgia? Epidemiology Misconceptions Associated with FM What Causes Fibromyalgia? Pathophysiology Why Is Fibromyalgia Challenging to Diagnose and Treat … and Does It Have to Be This Way? Approach to Diagnosis and Management Diagnosis of Fibromyalgia Criteria Overall Management of Fibromyalgia Pharmacotherapy Nonpharmacologic Options Support Systems Tracking Symptoms and Progress Patient-Centered Medical Homes (PCMHs) Conclusion Patient and Provider Resources Tools for Fibromyalgia Tracking Organizations and Support Groups Books Smartphone Apps References 6: Metabolic Bone Disease and Osteoporosis Osteoporosis Assessment for Fracture Risk and Osteoporosis The Limitation of DXA and Newer Techniques Treatment of Osteoporosis Combination and Sequential Treatments Secondary Osteoporosis Summary References 7: Crystal-Induced Arthritis Gout Presentation and Progression Cause Presentation Pitfalls and Pearls of Acute Monoarticular and Polyarticular Gout Natural History of Gout Acute Gout Chronic Tophaceous Gout Transplant-Associated Gout Treatment of Acute Gout NSAIDs, Colchicine, and Glucocorticoids Biologic Therapy Treatment of the Hyperuricemic State Allopurinol Febuxostat (Uloric) Uricosuric Drugs Uricases (Rasburicase, Pegloticase) Pitfalls and Pearls of Urate-Lowering Therapy (ULT) Comorbidities, Contraindications, and Therapeutic Choice Chronic Kidney Disease Hypertension Diabetes Mellitus and Hyperlipidemia Cardiovascular Disease Hepatic Impairment and Gastrointestinal Bleeding Drug Interactions When to Refer to the Rheumatologist Pitfalls and Pearls of Comorbidities Calcium Pyrophosphate Deposition Disease (CPPD) Presentation and Progression Cause Presentation Osteoarthritis and CPPD Disease Precipitators of Acute Pseudogout in the Elderly Diagnosis Natural History Treatment Agents That May Prevent Crystal Formation and Deposition in CPPD Magnesium Dietary Calcium Probenecid Phosphocitrate Hyaluronan Radiosynovectomy When to Refer Pearls and Pitfalls of CPPD Basic Calcium Phosphate (BCP) Crystal Deposition Disease Presentation and Progression Cause Presentation Diagnosis Expected Outcome Treatment Expected Response When to Refer Pearls and Pitfalls of BCP Summary References 8: Overuse Injuries Overuse Injuries Tendinopathy Epidemiology Pathophysiology Presentation/Symptoms Symptom Classification Physical Exam Diagnosis Treatment Stress Fractures Epidemiology Pathophysiology Presentation/Symptoms Physical Exam Diagnosis Treatment Periostitis and Periosteal-Muscle Junction Epidemiology Pathophysiology Presentation/Symptoms Physical Exam Example Images Diagnosis Treatment Peripheral Nerve Entrapment Epidemiology Pathophysiology Presentation/Symptoms Physical Exam Diagnosis Treatment Bursitis/Bursopathies Epidemiology Pathophysiology Presentation/Symptoms Physical Exam Diagnosis Treatment References 9: Systemic and Localized Inflammatory Diseases of Older Adults Inflammatory Arthritis Epidemiology, History, and Diagnosis Differential Diagnosis Treatment Polymyalgia Rheumatica and Giant Cell Arteritis Polymyalgia Rheumatica Giant Cell Arteritis Drug-Induced Lupus Localized Musculoskeletal Disorders Bursitis Spontaneous Osteonecrosis of the Knee (SONK) Diffuse Idiopathic Skeletal Hyperostosis (DISH) Discussion References 10: Interpretation of Rheumatological Tests Case Scenario Testing for Connective Tissue Diseases Systemic Lupus Erythematosus Antinuclear Antibodies Anti-Double-Stranded DNA Antibodies Anti-Smith Antibodies Drug-Induced Lupus Sjögren Syndrome Mixed Connective Tissue Disease Systemic Sclerosis (Scleroderma) Dermatomyositis and Polymyositis Rheumatoid Arthritis Rheumatoid Factor Anticyclic Citrullinated Peptide Antibodies Antineutrophil Cytoplasmic Antibody (ANCA)-Associated Vasculitis ANCA Other Tests Erythrocyte Sedimentation Rate C-Reactive Protein Human Leukocyte B27 Antigen Final Comment References 11: Infectious Arthritis Septic Arthritis Disseminated Gonococcal Infection Acute Rheumatic Fever Lyme Arthritis Chikungunya Virus Infection Parvovirus Infection Osteoarticular Tuberculosis References 12: Autoinflammatory Disease Introduction General Pathophysiology Diagnostic Clues for AIDs Familial Mediterranean Fever [18–20] Cryopyrin-Associated Periodic Syndrome [21–24] TNF Receptor-Associated Periodic Syndrome [16, 25, 26] Hyper-IgD Syndrome/Mevalonate Kinase Deficiency [27–29] NOD2-Associated Diseases Blau Syndrome Yao Syndrome [37–40] References 13: Scleroderma Patient Case Introduction Epidemiology Mechanisms/Pathophysiology Inflammation and Autoimmunity Vasculopathy Fibrosis Diagnosis and Screening Identifying Specific Clinical Features of Scleroderma Skin Sclerosis Raynaud’s Phenomenon Abnormal Nailfold Capillaries Fingertip Lesions: Cutaneous Ulcers Telangiectasia Pulmonary Hypertension Interstitial Lung Disease Scleroderma-Related Autoantibodies Identifying Other Important Signs and Symptoms of Scleroderma (Not Included in the 2013 ACR/EULAR Classification Criteria) Gastrointestinal Dysmotility and Vasculopathy Cardiac Involvement Scleroderma Renal Crisis Skin Calcinosis An Algorithmic Approach to the Diagnosis of Scleroderma Staging and Management Skin Sclerosis Raynaud’s Phenomenon Pulmonary Hypertension Interstitial Lung Disease Gastrointestinal Dysmotility Scleroderma Renal Crisis Quality of Life in Scleroderma Risk of Malignancy and Associated Autoimmune Conditions Referral Guidelines and Outlook Conclusion/Case Summary References 14: Vasculitis Introduction Large-Vessel Vasculitis Giant Cell Arteritis Epidemiology Clinical Features and Findings Diagnosis Treatment Takayasu’s Arteritis Epidemiology Clinical Features and Findings Diagnosis Treatment Medium-Vessel Vasculitis Polyarteritis Nodosa Epidemiology Clinical Features and Findings Diagnosis Treatment Small-Vessel Vasculitis ANCA-Associated Vasculitis Granulomatosis with Polyangiitis Epidemiology Clinical Features and Findings Diagnosis Treatment Microscopic Polyangiitis Epidemiology Clinical Features and Findings Diagnosis Treatment Eosinophilic Granulomatosis with Polyangiitis Epidemiology Clinical Features and Findings Diagnosis Treatment Cryoglobulinemic Vasculitis Epidemiology Clinical Features and Findings Diagnosis Treatment Behcet’s Syndrome Epidemiology Clinical Features and Findings Diagnosis Treatment Paraneoplastic Vasculitis Relevant Comorbidities References 15: Ankylosing Spondylitis Epidemiology Etiology and Pathogenesis Genetic Factors Intestinal Dysbiosis Clinical Features Musculoskeletal Manifestations Extra-Articular Manifestations Complications Diagnosis History Physical Exam Spinal Mobility Laboratory Tests Imaging Treatment Initial Therapy Nonpharmacologic Interventions Pharmacologic Therapy NSAID Nonresponders When to Consider Tapering Biologic Therapy When to Consider Switching a Biologic Agent Resistant to Standard Therapies Management of Extra-Articular Manifestations Surgery Considerations in Preoperative Clearance of AS Patients Risk of COVID-19 in AS Patients Prognosis Prognostic Indicators Conclusions References Index